Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
Anthos Therapeutics' Abelacimab, a Factor XI/XIa inhibitor, demonstrated a 67% reduction in major or clinically relevant non-major bleeding compared to Rivaroxaban in atrial fibrillation patients
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3 min read
Anthos Therapeutics' Abelacimab, a Factor XI/XIa inhibitor, demonstrated a 67% reduction in major or clinically relevant non-major bleeding compared to Rivaroxaban in atrial fibrillation patients
20 November 2023
Abelacimab 150 mg, a unique Factor XI/XIa inhibitor from Anthos Therapeutics, showcased a 67% decline in significant or notably relevant non-major bleeding versus Rivaroxaban in atrial fibrillation patients.
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An analysis of Atezolizumab's R&D progress and its clinical results presented at the 2023 AACR Annual Meeting
An analysis of Atezolizumab's R&D progress and its clinical results presented at the 2023 AACR Annual Meeting
20 November 2023
On 15 Apr 2023, the efficacy and safety of adjuvant (adj) atezolizumab (atezo) from the Phase 2 LCMC3 study was reported at the AACR Congress.
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Satralizumab Unveiled: A Detailed Overview of its Revolutionary R&D Breakthroughs
Drug Insights
4 min read
Satralizumab Unveiled: A Detailed Overview of its Revolutionary R&D Breakthroughs
20 November 2023
This article summarized the latest R&D progress of Satralizumab, the Mechanism of Action for Satralizumab, and the drug target R&D trends for Satralizumab.
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Novartis research indicates that the oral drug remibrutinib can start easing chronic spontaneous urticaria symptoms by week two of treatment
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Novartis research indicates that the oral drug remibrutinib can start easing chronic spontaneous urticaria symptoms by week two of treatment
20 November 2023
Novartis research suggests that remibrutinib, an oral medication, can effectively ease symptoms of chronic spontaneous urticaria as early as the second week of treatment.
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Paclitaxel: brief review of its R&D progress and the clinical result in 2023 ESMO
ESMO 2023
4 min read
Paclitaxel: brief review of its R&D progress and the clinical result in 2023 ESMO
20 November 2023
On 23 Oct 2023, the updated results of a phase II clinical trial: Paclitaxel and carboplatin plus PD-1 blockades combined with anlotinib as first-line treatment for advanced oesophageal cancer was reported at the ESMO Congress.
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Ocugen declares commencement of Phase 1/2 trial after first administration on patient for OCU410ST
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Ocugen declares commencement of Phase 1/2 trial after first administration on patient for OCU410ST
20 November 2023
Ocugen, Inc. declares commencement of Phase 1/2 trial after first administration on patient for OCU410ST - a modifier gene therapy for Stargardt Disease, assessing its safety and effectiveness.
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 Unleashing the Power of Sevelamer Hydrochloride: A Comprehensive Review on R&D Breakthroughs
Drug Insights
4 min read
Unleashing the Power of Sevelamer Hydrochloride: A Comprehensive Review on R&D Breakthroughs
20 November 2023
This article summarized the latest R&D progress of Sevelamer Hydrochloride, the Mechanism of Action for Sevelamer Hydrochloride, and the drug target R&D trends for Sevelamer Hydrochloride.
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Sana Biotech Reveals FDA Approval of New Drug Application for SC291
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Sana Biotech Reveals FDA Approval of New Drug Application for SC291
20 November 2023
Sana Biotech Reveals FDA Approval of New Drug Application for SC291, a Hypoimmune-modified, Targeting CD19, Allogeneic CAR T Treatment, Targeted for Lupus Nephritis, Extrarenal Lupus, and ANCA-linked Vasculitis Patients.
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Fam-trastuzumab deruxtecan-NXKI: brief review of its R&D progress and the clinical result in 2023 ESMO
ESMO 2023
4 min read
Fam-trastuzumab deruxtecan-NXKI: brief review of its R&D progress and the clinical result in 2023 ESMO
20 November 2023
The disclosure of the clinical trial of Trastuzumab deruxtecan (T-DXd) for the pretreatment of patients (pts) with her2-expressing solid tumors at ESMO 2023 provides the factual basis for subsequent, more in-depth studies.
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The US FDA has approved Takeda's ADZYNMA for treating Congenital Thrombotic Thrombocytopenic Purpura (cTTP)
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The US FDA has approved Takeda's ADZYNMA for treating Congenital Thrombotic Thrombocytopenic Purpura (cTTP)
20 November 2023
US FDA has given the green light to Takeda's ADZYNMA (recombinant-krhn, ADAMTS13) for the management of Congenital Thrombotic Thrombocytopenic Purpura (cTTP).
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A Comprehensive Review of Spiramycin's R&D Innovations and Drug Target Mechanism
Drug Insights
4 min read
A Comprehensive Review of Spiramycin's R&D Innovations and Drug Target Mechanism
20 November 2023
This article summarized the latest R&D progress of Spiramycin, the Mechanism of Action for Spiramycin, and the drug target R&D trends for Spiramycin.
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Boston Pharma unveils positive Phase 2a data for monthly NASH drug BOS-580, highlighting effects on diabetics, at 2023 AASLD Liver Meeting
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3 min read
Boston Pharma unveils positive Phase 2a data for monthly NASH drug BOS-580, highlighting effects on diabetics, at 2023 AASLD Liver Meeting
20 November 2023
Boston Pharma shares promising Phase 2a results for potential once-a-month BOS-580 treatment in NASH and its impact on diabetic groups, showcased at the 2023 AASLD Liver Meeting.
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